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Hemoglobin
international journal for hemoglobin research
Volume 33, 2009 - Issue 6
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Short Communications

Detection of a Rare Mutation in An Iranian Family: Codons 37/38/39 (7 bp Deletion)

Azita Zadeh-Vakili Thalassemia Prenatal Diagnosis Center, Ali Asghar Hospital, Zahedan University of Medical Sciences, Zahedan, IranCorrespondence[email protected]
&
Payman Eshghi Department of Pediatrics Hematology-Oncology, Mofid Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Pages 523-527 | Received 17 May 2009, Accepted 29 Jun 2009, Published online: 03 Dec 2009

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